Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 43

Cited In for PubMed (Select 17579608)


DISC1 (disrupted-in-schizophrenia-1) regulates differentiation of oligodendrocytes.

Hattori T, Shimizu S, Koyama Y, Emoto H, Matsumoto Y, Kumamoto N, Yamada K, Takamura H, Matsuzaki S, Katayama T, Tohyama M, Ito A.

PLoS One. 2014 Feb 7;9(2):e88506. doi: 10.1371/journal.pone.0088506. eCollection 2014.


Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes.

Mullin AP, Gokhale A, Moreno-De-Luca A, Sanyal S, Waddington JL, Faundez V.

Transl Psychiatry. 2013 Dec 3;3:e329. doi: 10.1038/tp.2013.108. Review.


Role of disrupted in schizophrenia 1 (DISC1) in stress-induced prefrontal cognitive dysfunction.

Gamo NJ, Duque A, Paspalas CD, Kata A, Fine R, Boven L, Bryan C, Lo T, Anighoro K, Bermudez L, Peng K, Annor A, Raja A, Mansson E, Taylor SR, Patel K, Simen AA, Arnsten AF.

Transl Psychiatry. 2013 Dec 3;3:e328. doi: 10.1038/tp.2013.104.


Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome.

Campbell MG, Kohane IS, Kong SW.

BMC Med Genomics. 2013 Sep 24;6:34. doi: 10.1186/1755-8794-6-34.


Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

Tropeano M, Ahn JW, Dobson RJ, Breen G, Rucker J, Dixit A, Pal DK, McGuffin P, Farmer A, White PS, Andrieux J, Vassos E, Ogilvie CM, Curran S, Collier DA.

PLoS One. 2013 Apr 18;8(4):e61365. doi: 10.1371/journal.pone.0061365. Print 2013.


Parental psychiatric disorders and autism spectrum disorders.

Jokiranta E, Brown AS, Heinimaa M, Cheslack-Postava K, Suominen A, Sourander A.

Psychiatry Res. 2013 May 30;207(3):203-11. doi: 10.1016/j.psychres.2013.01.005. Epub 2013 Feb 4.


DISC1 as a therapeutic target for mental illnesses.

Hikida T, Gamo NJ, Sawa A.

Expert Opin Ther Targets. 2012 Dec;16(12):1151-60. doi: 10.1517/14728222.2012.719879. Epub 2012 Nov 6. Review.


A review of the evidence for the canonical Wnt pathway in autism spectrum disorders.

Kalkman HO.

Mol Autism. 2012 Oct 19;3(1):10. doi: 10.1186/2040-2392-3-10.


The BTBR T+ tf/J mouse model for autism spectrum disorders-in search of biomarkers.

Meyza KZ, Defensor EB, Jensen AL, Corley MJ, Pearson BL, Pobbe RL, Bolivar VJ, Blanchard DC, Blanchard RJ.

Behav Brain Res. 2013 Aug 15;251:25-34. doi: 10.1016/j.bbr.2012.07.021. Epub 2012 Aug 9. Review.


The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.

Strug LJ, Addis L, Chiang T, Baskurt Z, Li W, Clarke T, Hardison H, Kugler SL, Mandelbaum DE, Novotny EJ, Wolf SM, Pal DK.

PLoS One. 2012;7(7):e40696. doi: 10.1371/journal.pone.0040696. Epub 2012 Jul 18.


Mice with reduced NMDA receptor expression: more consistent with autism than schizophrenia?

Gandal MJ, Anderson RL, Billingslea EN, Carlson GC, Roberts TP, Siegel SJ.

Genes Brain Behav. 2012 Aug;11(6):740-50. doi: 10.1111/j.1601-183X.2012.00816.x.


DISC1 and Striatal Volume: A Potential Risk Phenotype For mental Illness.

Chakravarty MM, Felsky D, Tampakeras M, Lerch JP, Mulsant BH, Kennedy JL, Voineskos AN.

Front Psychiatry. 2012 Jun 19;3:57. doi: 10.3389/fpsyt.2012.00057. eCollection 2012.


Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions.

Ameis SH, Szatmari P.

Front Psychiatry. 2012 May 15;3:46. doi: 10.3389/fpsyt.2012.00046. eCollection 2012.


DISC1 Pathway in Brain Development: Exploring Therapeutic Targets for Major Psychiatric Disorders.

Kamiya A, Sedlak TW, Pletnikov MV.

Front Psychiatry. 2012 Mar 22;3:25. doi: 10.3389/fpsyt.2012.00025. eCollection 2012.


Aggregated proteins in schizophrenia and other chronic mental diseases: DISC1opathies.

Korth C.

Prion. 2012 Apr-Jun;6(2):134-41. doi: 10.4161/pri.18989. Epub 2012 Apr 1. Review.


Linking neurodevelopmental and synaptic theories of mental illness through DISC1.

Brandon NJ, Sawa A.

Nat Rev Neurosci. 2011 Nov 18;12(12):707-22. doi: 10.1038/nrn3120. Review.


Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

Moens LN, De Rijk P, Reumers J, Van den Bossche MJ, Glassee W, De Zutter S, Lenaerts AS, Nordin A, Nilsson LG, Medina Castello I, Norrback KF, Goossens D, Van Steen K, Adolfsson R, Del-Favero J.

PLoS One. 2011;6(8):e23450. doi: 10.1371/journal.pone.0023450. Epub 2011 Aug 11.


Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders.

Liu XQ, Georgiades S, Duku E, Thompson A, Devlin B, Cook EH, Wijsman EM, Paterson AD, Szatmari P.

J Am Acad Child Adolesc Psychiatry. 2011 Jul;50(7):687-696.e13. doi: 10.1016/j.jaac.2011.05.002.


Maternal genetic mutations as gestational and early life influences in producing psychiatric disease-like phenotypes in mice.

Gleason G, Zupan B, Toth M.

Front Psychiatry. 2011 May 11;2:25. doi: 10.3389/fpsyt.2011.00025. eCollection 2011.


Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesis.

Stephenson DT, O'Neill SM, Narayan S, Tiwari A, Arnold E, Samaroo HD, Du F, Ring RH, Campbell B, Pletcher M, Vaidya VA, Morton D.

Mol Autism. 2011 May 16;2(1):7. doi: 10.1186/2040-2392-2-7.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk